3. 1. References
ā¢ Medscape
ā¢ Up-to-Date
ā¢ WHO Publication
ā¢ Dengue Case Management
ā¢ CWM ED CME Presentation
ā¢ Journal articles
ā¢ Tropical Medicine and Intā Health (2001, 2004)
ā¢ Indian Journal of Pediatrics (2006)
ā¢ Clinical Microbiology Review (2009)
4. 2. Introduction
ā¢ The most common arbovirus globally
ā¢ Tropics at risk (approx. 2.5-3 Billion)
ā¢ 4 distinct serotypes (1-4)
ā¢ Flavivirus (ss RNA)
ā¢ Vector-borne (Genus Aedes) but other routes possible
ā¢ Common species are aegypti, albopictus and
polynesiensis.
ā¢ Transmission/ Outbreak patterns
ā¢ Usually self limiting, MR <1%,
6. 4. Classification
Infection
Asymptomatic Symptomatic
Undifferentiated Dengue Fever
NO Warning
Signs
Severe Dengue
With Warning
Signs
50-90%
7. 4. Classification (II)
ā¢ Dengue fever without warning signs
ā¢ Hx of being in endemic area.
ā¢ Fever and 2 of the following
ā¢ Aches and pains
ā¢ Nausea & vomitting
ā¢ Rash
ā¢ Tourniquet test positive
ā¢ Leukopenia
9. 4. Classifications (IV)
ā¢ Severe Dengue
1. Severe plasma leakage leading to
ā¢ Shock
ā¢ Fluid accumulation with respiratory distress
2. Severe bleeding as evidenced by a doctor
3. Severe organ involvement
ā¢ Liver: AST or ALT >1000
ā¢ CNS: Impaired consciousness
ā¢ Heart and other organ dysfunctions
10. 5. Clinical Course
ā¢ Incubation period (3-7 days)
ā¢ Febrile phase (2-7 days)
ā¢ Critical phase (1-3 days)
ā¢ Marked by defervescence , leukopenia and
thrombocytopenia.
ā¢ Recovery phase (or Severe Dengue.)
ā¢ May have bradycardia. Important to avoid fluid
overload!
ā¢ Patients can and will present in any of the 3 stages so good
history and timeline is critical to know where the patient
stands and what to expect next.
11. 5. Clinical Course (II)
ā¢ Severe Dengue
ā¢ Recognising shock is important. Case fatality as
high 12%
ā¢ Usually on day 4/5 of illness.
ā¢ Pulse pressure is <20mmHg
ā¢ Poor capillary perfusion
ā¢ Cold extremities
ā¢ Delayed cap. Refill
ā¢ Tachycardia
ā¢ Hypotension is often a late sign
12. 6. Assessment
ā¢ History
ā¢ Important to determine timeline, family history and
past infections in mother for infants.
ā¢ N.B. Maternal antibodies only protect for first 6 months.
ā¢ Physical Exam
ā¢ Vitals must be carefully observed and mental state
ā¢ Tourniquet test (>20 petechiae/inch2)
ā¢ Usu. Non-specific but maculopapular rash,
conjunctival injection, pharyngeal oedema,
lymphadenopathy and hepatomegaly may be seen in
upto 50% of cases.
13. 7. Investigations
ā¢ Serology:
ā¢ Within 3 days NS1 Strip test
ā¢ > 3days IgM (Potential for false positive present for 6 days
though)
ā¢ IgG will indicate secondary infection (A fourfold titre increase is
needed)
ā¢ Bloods
ā¢ FBC- Leukopenia, Changes in HCT.
ā¢ PLT- <150,000
ā¢ Peripheral blood smear- Transformed lymphocytes
ā¢ Albumin- low due to extravasation
ā¢ Liver function tests
ā¢ Urine output
ā¢ CXR, AXR, USS- to pick up fluid accumulation
14. 8. Differentials
Febrile Stage
ā¢ Leptospirosis
ā¢ Measles
ā¢ Typhoid
ā¢ Malaria
Critical Phase
ā¢ AFI
ā¢ As before
ā¢ Surgical
ā¢ Acute abdomen
ā¢ Upper GI Bleed
Use the timeline to differentiate. And these factors
favour Dengue: High fever, rash, retro-orbital pain
thrombocytopenia, leukopenia, absence of cough, and
absence of sore-throat.
15. 9. Management
Steps to take
1. Diagnosis, and classification of phase and
severity
2. Deciding if to be sent home, inpatient or
emergency referral and treatment.
3. Disease notification
16. 9. Management (II)
ā¢ Group A- Outpatient
ā¢ No warning signs
ā¢ Stable socio-economic status
ā¢ Group B- Inpatient
ā¢ Warning signs
ā¢ Infants
ā¢ Poor socio-economic situation
ā¢ Malnutrition, concurrent infections
ā¢ Group C- Emergency Inpatient
ā¢ Severe dengue- Plasma leakage, shock, fluid
accumulation, severe bleeds, organ impairment.
17. 9. Management (III)
Group A
ā¢ As doctor/clinic
ā¢ ORS, PCT, Bedrest, Vigilance
ā¢ Schedule daily followups. Monitor FBC, dehydration,
warning signs and defervescence
ā¢ Family advice
ā¢ Control fever (PCT 10-15mg/kg Q6H)
ā¢ Prevent dehydration
ā¢ Prevent spread within household
ā¢ Watch for warning signs as temp drops after 3-8 days.
18. 9. Management (IV)
Group B
ā¢ Admit. Assess fluid status, FBC and vitals every 4 hours
ā¢ Continually monitor for shock and severe dengue
ā¢ IV fluids- Crystalloids at 6ml/kg/hr first 2 hours and then
reassess and drop to 2-3ml/kg/hr. Maintain urine output
and perfusion. Usu. Will pass soon into recovery or
severe dengue.
ā¢ If HCT and BP stable reduce fluids
ā¢ If patient worsens increase to 20ml/kg for 1 hour and
assess.
ā¢ If danger signs picked up proceed to Group C
management
19. 9. Management (V)
Group C- Compensated Shock
ā¢ Admit to PICU or NICU
ā¢ Obtain investigations, assess fluid status and monitor
vitals as per ward protocol
ā¢ Fluid: 20ml/kg crystalloid over 1 hour and reduce to
10ml/kg for next hour if responsive and then 2-
3ml/kg/hr for next 6-8 hours.
ā¢ If not improving, change to colloid solution 10-15ml/kg
over 1 hour. Revert to crystalloids asap
ā¢ Once signs of reabsorbtion seen (bradycardia, rash) taper
fluids down to maintenance levels to prevent
hypervolaemia.
20. 9. Management (VI)
Group C- Hypotensive Shock or Hemorrhagic
ā¢ Admit to Nice or PICU, resuscitate as before.
ā¢ If after colloids patient still deteriorates (HCT,
etc) transfusion ma be necessary, if HCT drops
sharply.
ā¢ 5-10ml whole blood slowly over 2-4 hours and
monitor HCT.
ā¢ Avoid IM injections and movement to prevent
further bleeding
21. 9. Management (VII)
Fluid Overload
ā¢ Signs
ā¢ Resp. distress
ā¢ Cyanosis
ā¢ Ascitis
ā¢ Periorbital or soft tissue oedema
ā¢ Treatment
ā¢ Inotropic agents may be needed with small colloid
boluses. Avoid diuretics
ā¢ Aspirating large effusions
ā¢ PPV before pulmonary oedema develops
22. 9. Management (VIII)
Discharge Criteria
ā¢ Clinically
ā¢ No fever for 48 hours
ā¢ Gen. well-being, appetite, hemodynamic status, urine
output all improved and no respiratory distress
ā¢ Labs
ā¢ Increasing trend of platelets
ā¢ Stable HCT without intravenous fluids.
23. 10. Additional Points
ā¢ Atypical presentations make for worse prognosis .
ā¢ Interestingly, the latest outbreak in Fiji saw a rise in Guillain-
Barre syndrome. Currently under investigation.
ā¢ Children with suspected dengue can deteriorate very fast and
a high index of suspicion is needed on our part.
ā¢ Plasma leakage is the most specific and life-threatening
feature of severe dengue. Watch for the critical period
carefully (Deferevescence) and donāt overload with fluid.
ā¢ Primary prevention is the way out as vaccines are not
approved yet. Commedās important afterall! ļ
24. 11. References
ā¢ Medscape
ā¢ Up-to-Date
ā¢ WHO Publication
ā¢ Dengue Case Management
ā¢ CWM ED CME Presentation
ā¢ Journal articles
ā¢ Tropical Medicine and Intā Health (2001, 2004)
ā¢ Indian Journal of Pediatrics (2006)
ā¢ Clinical Microbiology Review (2009)
The End
Editor's Notes
After an incubation period of 2 to 7 days, the typical patient experiences the sudden onset of fever, headache, retroorbital pain, and back pain along with the severe
myalgia that gave rise to the colloquial designation "break-bone fever." There is often a macular rash on the first day as well as adenopathy, palatal vesicles, and
scleral injection. The illness may last a week, with additional symptoms usually including anorexia, nausea or vomiting, marked cutaneous hypersensitivity, and ā
near the time of defervescence ā a maculopapular rash beginning on the trunk and spreading to the extremities and head.